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Structure paper

TitleIndolo-Phakellins as beta 5-Specific Noncovalent Proteasome Inhibitors.
Journal, issue, pagesAngew. Chem. Int. Ed. Engl., Vol. 54, Page 2830-2833, Year 2015
Publish dateNov 21, 2014 (structure data deposition date)
AuthorsBeck, P. / Lansdell, T.A. / Hewlett, N.M. / Tepe, J.J. / Groll, M.
External linksAngew. Chem. Int. Ed. Engl. / PubMed:25581903
MethodsX-ray diffraction
Resolution2.5 Å
Structure data

PDB-4rur:
Yeast 20S proteasome in complex with the alkaloid indolo-phakellin (4)
Method: X-RAY DIFFRACTION / Resolution: 2.5 Å

Chemicals

ChemComp-MG:
Unknown entry

ChemComp-3WE:
(2E,3aR,14aS)-9-bromo-2-imino-1,2,3,5,6,14a-hexahydro-4H,8H-imidazo[4',5':5,6]pyrrolo[1',2':4,5]pyrazino[1,2-a]indol-8-one

ChemComp-HOH:
WATER

Source
  • saccharomyces cerevisiae s288c (yeast)
  • saccharomyces cerevisiae (brewer's yeast)
KeywordsHYDROLASE/HYDROLASE INHIBITOR / Proteasome / Alkaloid / Reversible Inhibition / Drug Discovery / Halogen Bonding / HYDROLASE-HYDROLASE INHIBITOR complex

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